"69452-130-30" National Drug Code (NDC)

Glimepiride 500 TABLET in 1 BOTTLE (69452-130-30)
(Bionpharma Inc.)

NDC Code69452-130-30
Package Description500 TABLET in 1 BOTTLE (69452-130-30)
Product NDC69452-130
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20151001
End Marketing Date20200229
Marketing Category NameANDA
Application NumberANDA091220
ManufacturerBionpharma Inc.
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]

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